Erratum to “Detection of rarely identified multiple mutations inMECP2gene do not contribute to enhanced severity in Rett syndrome”, Am J Med Genet Part A 161A:1638-1646-Reference-Cited by-同舟云学术

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Erratum to “Detection of rarely identified multiple mutations inMECP2gene do not contribute to enhanced severity in Rett syndrome”, Am J Med Genet Part A 161A:1638-1646

Published:2014-04-14 Issue:5 Volume:164 Page:1346-1346
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet

Author:

Chapleau Christopher A.¹,Lane Jane²,Kirwin Susan³,Schanen Carolyn³,Vinette Kathy M. B.³,Stubbolo Danielle³,MacLeod Patrick⁴,Glaze Daniel G.⁵,Motil Kathleen J.⁵,Neul Jeffrey L.⁶,Skinner Steven A.⁷,Kaufmann Walter E.⁸,Percy Alan K.²

Affiliation:

1. Department of Pharmacy; Civitan International Research Center, The University of Alabama at Birmingham; Birmingham Alabama

2. Department of Pediatrics; Civitan International Research Center, The University of Alabama at Birmingham; Birmingham Alabama

3. Biomedical Research Department; Nemours/Alfred I. duPont Hospital for Children; Wilmington Delaware

4. Division of Medical Genetics, Department of Pathology; Laboratory Medicine and Medical Genetics, Victoria General Hospital; Victoria Canada

5. Department of Pediatrics; Baylor College of Medicine; Houston Texas

6. Duncan Neurological Research Institute; Texas Children's Hospital and Baylor College of Medicine; Houston Texas

7. Greenwood Genetic Center; Greenwood South Carolina

8. Children's Hospital Boston; Harvard Medical School; Boston Massachusetts

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36493/fullpdf

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